Canonical Allele Identifier: CA2014026233

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333777G= , CM000674.2:g.6333777G=	GRCh38
NC_000012.11:g.6442943G= , CM000674.1:g.6442943G=	GRCh37
NC_000012.10:g.6313204G=	NCBI36
NG_007506.1:g.13319C= , LRG_193:g.13319C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.282C= MANE Select	NP_001056.1:p.Asn94=
ENST00000162749.7:c.282C= MANE Select	ENSP00000162749.2:p.Asn94=
NM_001065.3:c.282C= , LRG_193t1:c.282C=	NP_001056.1:p.Asn94=
NM_001346091.1:c.-43C=	NP_001333020.1:n.-43C=
NM_001346091.2:c.-43C=	NP_001333020.1:n.-43C=
NM_001346092.1:c.-296C=	NP_001333021.1:n.-296C=
NM_001346092.2:c.-296C=	NP_001333021.1:n.-296C=
NR_144351.1:n.585C=
NR_144351.2:n.544C=
ENST00000162749.6:c.282C=	ENSP00000162749.2:p.Asn94=
ENST00000366159.8:c.282C=	ENSP00000380389.3:p.Asn94=
ENST00000366159.9:n.316C=
ENST00000437813.7:n.243C=
ENST00000437813.8:c.282C=	ENSP00000513672.1:p.Asn94=
ENST00000440083.6:c.282C=	ENSP00000413224.2:p.Asn94=
ENST00000440083.7:c.282C=	ENSP00000413224.3:p.Asn94=
ENST00000534885.5:c.128C=	ENSP00000441803.1:p.Thr43=
ENST00000535958.1:n.528C=
ENST00000535958.2:c.*109C=	ENSP00000513673.1:n.*109C=
ENST00000536194.1:c.255C=	ENSP00000442919.1:p.Asn85=
ENST00000539372.5:c.282C=	ENSP00000442059.1:p.Asn94=
ENST00000540022.5:c.194-261C=	ENSP00000438343.1:n.194-261C=
ENST00000543048.5:c.214+68C=	ENSP00000439981.1:n.214+68C=
ENST00000543995.5:c.193+314C=	ENSP00000442405.1:n.193+314C=
ENST00000698339.1:c.282C=	ENSP00000513670.1:p.Asn94=
ENST00000698340.1:c.282C=	ENSP00000513671.1:p.Asn94=